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UNKNOWN STEM Adverse Event — Injury (MDR 0001822565-2020-01477)

UNKNOWN STEM Adverse Event — Injury (MDR 0001822565-2020-01477) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN STEM; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER BIOMET, INC..

DeviceUNKNOWN STEM
Generic namePROSTHESIS, HIP
ManufacturerZIMMER BIOMET, INC.
Report number0001822565-2020-01477
Event typeInjury
Product problemN
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, DISTRI
Narrative(B)(4). EVENT DATE (B)(6) 2020. EXPLANT DATE (B)(6) 2020. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION PROVIDED BY THE CUSTOMER. DHR WAS UNABLE TO BE REVIEWED AS THE LOT NUMBER FOR THE DEVICE IS UNKNOWN. THE ROOT CAUSE IS UNABLE TO BE DETERMINED.
SourceopenFDA MAUDE (device adverse events)

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